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10q11.2

A chromosome band present on 10q
National Institutes of Health

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9 relations
10qALOX5 wt AlleleChromosomesDKK1 wt Allele

Papers overview

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Highly Cited
2009
Highly Cited
2009
Fine mapping and functional analysis of a common variant in MSMB on chromosome 10q11.2 associated with prostate cancer susceptibility
Two recent genome-wide association studies have independently identified a prostate cancer susceptibility locus on chromosome… 
Highly Cited
2003
Highly Cited
2003
Germline PTEN promoter mutations and deletions in Cowden/Bannayan-Riley-Ruvalcaba syndrome result in aberrant PTEN protein and dysregulation of the phosphoinositol-3-kinase/Akt pathway.
Germline intragenic mutations in PTEN are associated with 80% of patients with Cowden syndrome (CS) and 60% of patients with… 
Highly Cited
1999
Highly Cited
1999
Pharmacogenetic association between ALOX5 promoter genotype and the response to anti-asthma treatment
Clinically similar asthma patients may develop airway obstruction by different mechanisms. Asthma treatments that specifically… 
Review
1999
Review
1999
RET proto-oncogene in the development of human cancer.
  • C. Eng
  • Journal of Clinical Oncology
  • 1999
  • Corpus ID: 40658036
The RET proto-oncogene, located on chromosome subband 10q11.2, encodes a receptor tyrosine kinase expressed in tissues and tumors… 
Highly Cited
1995
Highly Cited
1995
Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung disease.
Hirschsprung disease (HSCR) is a common congenital malformation (1 in 5,000 live births) due to the absence of autonomic ganglia… 
Highly Cited
1994
Highly Cited
1994
Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease
HIRSCHSPRUNG'S disease is a genetic disorder of neural crest development affecting 1 in 5,000 births. It is characterized by the… 
Highly Cited
1994
Highly Cited
1994
Mutations of the RET proto-oncogene in Hirschsprung's disease
HIRSCHSPRUNG'S disease (HSCR)1 is a common condition (1 in 5,000 live births) resulting in intestinal obstruction in neonates2… 
Highly Cited
1994
Highly Cited
1994
Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours.
The susceptibility loci for the three multiple endocrine neoplasia (MEN) type 2 syndromes have been mapped to the region of… 
Highly Cited
1992
Highly Cited
1992
Single base polymorphism at −511 in the human interleukin-1β gene (IL1β)
F.S. di Giovine*. E.Takhsh, A.I.F.BIakemore and G.W.Duff Section of Molecular Medicine, Department of Medicine and Pharmacology… 
Highly Cited
1989
Highly Cited
1989
Human ret proto-oncogene mapped to chromosome 10q11.2.
Using cosmid clones derived from human ret protooncogene as probes, we determined its chromosome localization by fluorescence in… 
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